NCT03689205

Brief Summary

Before surgery, patients will fill the Beck anxiety, distress tolerance test and Pain katastrophizing test. Patients will be divided into two groups according to BMI\> 30kg / m2 (Group A) and BMI \<30kg / m2 (Group B). Compared to body weight, venous vascular pain of the groups will be compared.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
70

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jun 2018

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 20, 2018

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

September 27, 2018

Completed
1 day until next milestone

First Posted

Study publicly available on registry

September 28, 2018

Completed
22 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 20, 2018

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

November 20, 2018

Completed
Last Updated

September 28, 2018

Status Verified

September 1, 2018

Enrollment Period

4 months

First QC Date

September 27, 2018

Last Update Submit

September 27, 2018

Conditions

PainCannulationBody Mass Index

Outcome Measures

Primary Outcomes (1)

  • Visual analog scale

    pain intensity

    one month

Study Arms (2)

Patients that BMI> 30kg / m2 (Group A)

Venous puncture pain on patients that Body mass index \> 30kg / m2

Patients that BMI< 30kg / m2 (Group B)

Venous puncture pain on patients that Body mass index \< 30kg / m2

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

After surgery patients

You may qualify if:

  • American Society of Anesthesiologist (ASA) physical status 1 and 2, between the ages of 18 and 65, were scheduled for elective surgery

You may not qualify if:

  • Patients with a history of anxiety disorders or hearing problem and preoperative pain, emergency surgery

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Gaziosmanpasa University

Tokat Province, 60200, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Pain

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Hakan Tapar

    Gaziosmanpasa University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Hakan Tapar

CONTACT

03562129500hakantapar@hotmail.com

Hakan Tapar

CONTACT

03562129500akantapar@hotmail.com

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assist. Prof

Study Record Dates

First Submitted

September 27, 2018

First Posted

September 28, 2018

Study Start

June 20, 2018

Primary Completion

October 20, 2018

Study Completion

November 20, 2018

Last Updated

September 28, 2018

Record last verified: 2018-09

Locations

TU(1)